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Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women

Valuation of the Low Back Pain Treated With Different Types of Active Exercises in Women

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02103036
Acronym
ECOLUM
Enrollment
30
Registered
2014-04-03
Start date
2014-03-31
Completion date
2015-10-31
Last updated
2014-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Low Back Pain, Core stability exercise, Back school, TENS, Infra- red light

Brief summary

The purpose of the study is determine whether the Core Stability Exercise is more effective than the traditional Back School for low back pain (LBP) in women.

Detailed description

The aim of this study is to check what kind of exercises are the best to treat LBP with regard to clinical improvements. The secondary objectives are: to determine which treatment is more effective in improving pain in the fewest sessions possible, to determine the involvement of inflammatory biomarkers in the development of pain and revalue the results after one month of having finishing treatment. The project is a longitudinal, single-blind and randomized study with two treatment groups: GROUP 1: Infrared light+ Transcutaneous Electrical Nerve Stimulation (TENS) + Core Stability Exercises. GROUP 2: Infrared light + Transcutaneous Electrical Nerve Stimulation (TENS) + Traditional Back School. Duration of treatment: 4 weeks. The participants will performe the exercises in 20 daily sessions (Monday to Friday) guided by a physiotherapist. Following treatment with the physiotherapist, the participants should perform the exercises at home for 4 weeks at a rate of three times per week.

Interventions

The increase in intra-abdominal pressure stiffens and strengthens the relevant structural support around the spine, compacts the arthrogenic structures and in combination with abdominal contraction, it can encourage a rigid cylinder and stiffness to occur around the spine. The relevant anatomy in these type of exercises are deep muscles like transversus abdominous, multifidus or pelvic floor. The participants will have to do 10 different exercises. They will have to perform from 8 to 10 repetitions of every exercise, guided by a physical therapist. They will be recommended about making some series more at home, three days a week, when the treatment was finished.

PROCEDURETraditional Back School

The back school exercises are based in the traditional activity used for improve the back pain symptoms using the breathing with the stretching of the trunk muscles, the erector spinae reinforcement, the abdominal reinforcement or the postural movements. The participants will have to do 10 different exercises. They will have to perform from 8 to 10 repetitions of every exercise, guided by a physical therapist. They will be recommended about making some series more at home, three days a week, when the treatment was finished.

DEVICETENS

Used equipment: MEGASONIC 313 P4 (Carin). Application program number 15: analgesic TENS with stimulation of afferent fibers. Type of current: two-phase TNS. Width of the impulse: 70µs. Frequency of the impulse: 100Hz. Train: Not. Pause / pause activates: Not. Time of treatment: 20 minutes.

DEVICEInfra-red

Used equipment: INFRA - 2000 (Enraf Nonius) with the following parameters: 230 V / 50-60 Hz / 1.2 A

Sponsors

Hospital Universitari Sant Joan de Reus
CollaboratorOTHER
University Rovira i Virgili
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18 to 70 years. * Diagnosis of back pain from a trauma. * Untreated pain (except acetaminophen). * Informed consent.

Exclusion criteria

* Algic process in the lumbar spine of infectious, neoplastic, metastasis, osteoporosis, inflammatory arthritis or fractures. * Cognitive impairment of any etiology. * Exercise intolerance for any reason. * Patients who have completed physical therapy in the last 3 months. * Patients who have received infiltration injections in the last 6 weeks.

Design outcomes

Primary

MeasureTime frameDescription
Changes in Visual Scale Analogue (VAS)Pain was measured at the beginning of the study (session 0), and changes are evaluated again at sessions 10, 20, and 1 month later.The VAS scale represents the pain intensity on a line of 10 cm, and one end there are the words no pain and the other end the worst imaginable pain written the distance in centimetres from the no pain point to the place marked by the patient represents the intensity of pain.

Secondary

MeasureTime frameDescription
Changes in the Roland- Morris Disability QuestionnaireDisability was measured at the beginning of the study (session 0), and changes are evaluated again at sessions 10, 20, and 1 month later.It consists of 24 items, which reflect limitation in different activities of daily living attributed by the patient to LBP. The patient must mark each item that applies to her current status. Scoring is also simple and fast; each checked item receives a score of 1, so scores range between 0 (no disability caused by LBP) and 24 (the maximum possible disability).

Other

MeasureTime frameDescription
Questionnaire of Physical Activity (ClassAF)The physical activity will be measured at the beginning of the study (session 0).Is a method developed by the Health Department of the Catalan Government. The ClassAF is a comprehensive questionnaire which contains a few items (1-4) to measure the general level of Physical Activity, it is calculated in METS (basal metabolic expenditure: mlO2/kg.min) and it allows to classify people into physically active or physically inactive.
Changes in the biomarkers: Tumor Necrosis Factor (TNF-Alpha) and Interleukin 10 (IL-10)The concentrations of these biomarkers will be measured at the beginning (session 0) and changes will be evaluated again at the end of the treatment (session 20).These two cytokines are parameters to indicate the inflammation levels. Their concentrations are measured using commercial ELISA kits.

Countries

Spain

Contacts

Primary ContactRosa Nogués, Ph D.
mariarosa.nogues@urv.cat+34977759355
Backup ContactEduard Minobes, PT
eminobes@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026